GUDIDData
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gudid Primary ID: 10016413

CEDIA Cocaine Assay (UDI 10016413)

Manufactured by Microgenics Corporation

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CEDIA Cocaine Assay - Primary ID 10016413

Device Regulatory Overview

The CEDIA Cocaine Assay (Model/Catalog Number: 10016413) is a medical device manufactured by Microgenics Corporation. This product is indexed under FDA Product Code / Category Classification DIO within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 3 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-1284-2022 View Full Alert →

QMS Tacrolimus Immunoassay REF 10015573 CALIBRATOR SET QMS TACROLIMUS CAL A 10015566-3 QMS TACROLIMUS CAL B 10015567-3 QMS TACROLIMUS C...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
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ID: Z-1563-2013 View Full Alert →

Thermo Scientific MAS Bilirubin for Siemens and Dimension Vista Systems, , Product is manufactured and distributed by Microgenics Corporatio...

🔒 Compromised Lot & Serial Numbers Locked
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ID: Z-0379-2013 View Full Alert →

Thermo Scientific MAS Omni IMMUNE and Omni IMMUNE PRO; Liquid Assayed Integrated Immunoassay Control. Intended for use as an assayed con...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)

Technical Specifications

Model Number
10016413
Product Code / EMDN
DIO
Device Name
Database Sync Date
2026-08-09 09:45:39

Full Regulatory Attributes

🔒 Token Gated 
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of CEDIA Cocaine Assay?

The registered manufacturer of record for CEDIA Cocaine Assay is Microgenics Corporation.

What is the Primary UDI-DI identifier for CEDIA Cocaine Assay?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10016413.

What classification code is assigned to this device?

This device is registered under product classification code DIO.

Similar Classification Devices (DIO)

Other Devices by Microgenics Corporation

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint